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Hypohidrotic ectodermal dysplasia: a case report
Orbit, 2019Hypohidrotic ectodermal dysplasia is a common variation of ectodermal dysplasia, characterized by hypohidrosis (or anhidrosis), hypotrichosis, hypodontia, and other distinct facial features. Furthermore, ocular tissues of ectodermal origin may also be affected in this disease.
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Loose Anagen Hair in Hypohidrotic Ectodermal Dysplasia
Pediatrics International, 1996Abstract:We report a 4 year‐old boy affected with hypohidrotic ectodermal dysplasia in whom loose anagen hair syndrome (LAHS) was suspected clinically. The diagnosis was confirmed by examination of hair by optic and scanning electron microscopy. Loose anagen hairs have not been previously described in the ectodermal dysplasias.
Antoni Azón-Masoliver, Juan Ferrando
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A Genetic Study of Hypohidrotic Ectodermal Dysplasia
Pediatrics International, 1980AbstractThe heredity of hypohidrotic ectodermal dysplasia (HED) has been considered to be X‐linked recessive, autosomal recessive or autosomal dominant. In this report, a genetic analysis was carried out on a total of 57 patients with HED including 6 patients recently examined by the present authors and 51 patients reported in Japan before May, 1980 ...
Kunio Hayakawa, Takuya Ikeda, Shozo Ohdo
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Rapp‐Hodgkin hypohidrotic ectodermal dysplasia syndrome
Clinical Genetics, 1991Four members in three generations of a family had Rapp‐Hodgkin hypohidrotic ectodermal dysplasia syndrome with variable involvement of teeth, hair, nails and palate, characteristic facies and mild heat tolerance problems. In addition, the proband had a high sweat sodium, hypogenitalism, hypothelia and marked cicatricial scalp atrophy and scarring ...
Jack Goldblatt, Ian Walpole
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Hypohidrotic ectodermal dysplasia: clinical and molecular review
International Journal of Dermatology, 2018AbstractHypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. Although there are autosomal recessive and dominant forms, X‐linked (XL) is the most frequent form of the disease. This XL‐HED phenotype is associated with mutations in the gene encoding the transmembrane protein ectodysplasin‐1 ...
Claudia F. Méndez-Catalá +5 more
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Hypohidrotic ectodermal dysplasia with strabismus
The Journal of Dermatology, 2018Aoi Okubo +6 more
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(15) Hypohidrotic ectodermal dysplasia
British Journal of Dermatology, 1987openaire +2 more sources
HYPOHIDROTIC ECTODERMAL DYSPLASIA: UNUSUAL PALMPRINT IN A HETEROZYGOTE
British Journal of Dermatology, 2006openaire +3 more sources